Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
  • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
  • C09C3/12—Treatment with organosilicon compounds
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
  • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
  • C09C1/28—Compounds of silicon
  • C09C1/30—Silicic acid
  • C09C1/3081—Treatment with organo-silicon compounds
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/12—Surface area
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/20—Powder free flowing behaviour
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/90—Other properties not specified above

Definitions

• This invention relates to the surface-treated metallic-oxide fine powder, which has good flow ability and excellent stability against agitation time, and especially relates to a surface-treated silica fine powder. More specifically, this invention relates to the surface-treated metallic-oxide fine powder which improves the stability against agitation time, its production method, and an electrophotographic toner using the same, regarding the surface-treated silica fine powder etc., which is added in a powder coating, an electrophotographic toner, etc., in order to improve the flow ability, to prevent aggregation or to adjust charge, etc.
• the surface-treated metallic-oxide fine powder in which the surface of metallic-oxide fine powder, such as silica, titania, and alumina, is treated with organic materials, is widely used as the flow ability improving agent of the electrophotographic toner for a copying machine, a laser beam printer, and a plain-paper facsimile.
• the tribo-electro static charge to an iron powder and an iron oxide powder as a carrier is one of the important quality factors.
• the metallic-oxide powder which has negative charge in the tribo-electro static charge is general, the metallic-oxide powder which is controlled to positive charge is also known.
• a metallic-oxide powder having positive charge or zero charge, which is introduced with the amino group and the hydrophobic group is disclosed in Japanese Patent Laid Open No.62-185405.
• a method is shown in Japanese Patent Laid Open No.63-52561 in which the silica synthesized by a vapor phase method is treated with a silane containing epoxy groups and subsequently with the amines.
• the metallic-oxide powder, which was heated with the modified silicone oil containing epoxy groups, and treated with an organic compound containing amino group is shown in Japanese Patent Laid Open No.63-155155.
• the present invention solves the above-mentioned conventional problems, and provides the surface-treated metallic-oxide fine powder having excellent stability against agitation time as well as good flow ability.
• the metallic-oxide fine powder, especially silica fine powder, which has excellent stability against agitation time is obtained.
• a surface-treated powder is obtained in which the difference between the amounts of charge for 1 minute and 5 minutes is less than 200 ⁇ C/g, or the ratio of said amounts is less than 2.5.
• the surface-treated metallic-oxide fine powder of the present invention controls the charge of the metallic-oxide fine powder and improves the stability by suppressing the variation of the amount of charge with time by surface-treating with two silane coupling agents containing amino group, one of which is for controlling the charge and the other is for increasing the charge stability, and the hydrophobic agent and introducing plural kinds of amino groups and hydrophobic groups to the surface of the metallic-oxide fine powder.
• this invention relates to the surface-treated metallic-oxide fine powder which comprises the following formulations and its production method or use.
• humed silica As the surface-treated metallic-oxide fine powder of the present invention, especially as the silica fine powder, so-called humed silica can be used efficiently, which has the specific surface area (by nitrogen adsorption-process or BET process) of less than 400m 2 /g and was made by flame hydrolysis of a volatile silicon compound such as a silicon halide compound.
• AEROSIL50, 90G, 130, 200, 300, 380, 380S, TT600, OX50 can be used, which are the product names of NIPPON AEROSIL Co., Ltd. and on the market.
• the surface-treated metallic-oxide fine powder of the present invention is explained, taking a silica fine powder as an example.
• alumina powder and titanium oxide powder can be explained in the same way.
• the surface-treated silica powder of this invention stabilizes the tribo-electro static charge by surface-treating, using the silane coupling agent containing the primary amino group shown by the following formula 3, and at least one of the silane coupling agents containing amino group chosen from the silane coupling agents containing the amino group shown by the formula 4, and hydrophobic agent.
• X is the functional group which can be hydrolyzed
• R is the hydrogen group or the alkyl group
• the part of R1 and R2 can be replaced by nitrogen, oxygen or sulfur atom.
• n is an integer from 1 to 3
• m is an integer from 1 to 6.
• the hydrolysis groups represented by X are specifically a chloro group, an alkoxy group, an acetoxy group, a hydroxy group, etc.
• the silane coupling agent containing primary amino group shown by the above formula 3 mainly controls the charge and the following compounds are mentioned as specific examples. Although ⁇ -amino propyltrimethoxysilane, or ⁇ -amino propyltriethoxy-silane is preferable from the point of reactivity and kinds of sub-products, it is not limited to these compounds.
• silane coupling agent containing amino group shown by above formula 4 mainly improves the charge stability, and although the following compounds are mentioned as specific examples, it is not limited to these compounds.
• the addition amount of the silane coupling agent containing primary amino group of formula 3 is adjusted according to the specific surface area of the silica fine powder, 0.1 - 20 weight part is generally desirable to 100 weight part of the silica fine powder. Moreover, with respect to the addition amount of the silane coupling agent of formula 4, 0.1 to 20 weight part is desirable to 100 weight part of the silica fine powder.
• these amounts are under 0.1 weight parts, the controlling of the charge of the silica fine powder is not sufficient since there are few amounts of amino group introduced onto the surface of the silica fine powder, and good stability of the charge cannot be obtained.
• the amounts are more than 20 weight part, the silica fine powder itself becomes to show the hydrophilicity since the amino group is a hydrophilic functional group, and thus the hydrophobicity required as a toner additive cannot be obtained.
• any materials of the following can be used if they are general ones: the alkyl silazane compounds such as hexamethyldisilazane, the alkylalkoxy-silane compounds such as dimethylmethoxy-silane, dimethylethoxy-silane, trimethylmethoxysilane, methyltrimethoxy-silane, and butyltrimethoxy-silane, the chloro-silane compounds such as dimethyldichloro-silane and trimethylchloro-silane, the silicone varnish containing reactive functional groups, the non-reactive silicone varnish, the silicone oil containing reactive functional group, the non-reactive silicone oil, etc.
• the alkyl silazane compounds such as hexamethyldisilazane
• the alkylalkoxy-silane compounds such as dimethylmethoxy-silane, dimethylethoxy-silane, trimethylmethoxysilane, methyltrimethoxy-silane, and but
• the viscosity is less than 1000 cst. If the viscosity is 1000 cst or more, it is difficult to apply the surface-treated agent uniformly on the silica fine powder, and the aggregation of the silica fine powder may occur to give the bad influence on the tribo-electro static charge of the silica fine powder.
• hydrophobic agents are not limited specifically if they are general ones.
• hexamethyldisilazane or dimethylsiloxane is desirable in order to obtain high hydrophobicity.
• the addition amount of the hydrophobic agent is adjusted according to the specific surface area of the silica fine powder and the addition amount of the silane coupling agent containing amino group, the amount of 5 - 50 weight part of silane coupling agent containing amino group is desirable in general. If this amount is less than 5 weight part, high hydrophobicity cannot be obtained, on the other hand, even if the amount is more than 50 weight part, hydrophobicity is practically equal and the aggregation may rather increase, so that it is not desirable.
• the silica fine powder is charged into a container having a stirring equipment represented by a Henschel mixer etc., and is stirred under nitrogen atmosphere.
• the silane coupling agent containing primary amino group of the general formula 3, the silane coupling agent containing amino group of the general formula 4, and the hydrophobic agent are added to the stirred powder to be mixed uniformly, or these surface-treated agents are sprayed to the silica powder to be mixed uniformly.
• the addition order of the silane coupling agents of formula 3 and formula 4 is not limited.
• these surface-treated agents and silica powder After mixing these surface-treated agents and silica powder uniformly, they are heated for more than 30 minutes at a temperature of less than 300°C.
• the heating temperature is 300°C or higher, it is not desirable since the amino group introduced for controlling charge is heat decomposed, and it may cause the poor tribo-electro static charge and the coloring of the silica fine powder itself, etc.
• the hydrophobic surface-treated silica powder can be obtained, which improves the charge control and stability.
• a silica powder can be obtained wherein the tribo-electro static charge to iron powders satisfies at least one of the relational expressions shown in the following formula 1 or 2:
• silica powder synthesized by a vapor phase method (NIHON AEROSIL product; Aerosil 200) of 200 m 2 /g by BET specific surface area
• the mixed solution comprising 5g of ⁇ - aminopropyltriethoxy-silane (Shin-Etsu Chemical Co., Ltd. product: KBE 903) , N-( ⁇ - amino ethyl) - ⁇ - aminopropyltrimethoxy-silane (Shin-Etsu Chemical Co., Ltd. product: KBM603), and 15g of the dimethyl-silicone oil (Shin-Etsu Chemical Co., Ltd. product: KF 96) was sprayed to 100g of said silica powder. The sprayed powder was heated while being stirred for 60 minutes at 200°C, and then cooled to prepare the surface-treated silica fine powder A.
• NIHON AEROSIL product Aerosil 200
• Each mixed solution which consists of the silica powder synthesized by vapor pahse method having the specific surface areas shown in Table 1, the silane coupling agent containing primary amino group shown by the formula 3, the silane coupling agent containing amino group shown by the formula 4, and the hydrophobic agent, was used to prepare the surface-treated silica fine powders B to G by the same process as in Example 1 under the heating conditions shown in Table 1.
• Each mixed solution consisting of the silica powder synthesized by vapor phase method having the specific surface areas shown in Table 1, the silane coupling agent containing amino group shown by either of formula 3 or 4, and the hydrophobic agent, was used to be prepared the surface-treated silica fine powders H to J by the same process as in Example 1 under the heating conditions shown in Table 1.
• metallic-oxide fine powders such as silica with the small charge variation with time are provided.
• the powder such as silica has the small charge variation with time, and is suitable as the additive of the powder coatings or the electrophotographic toner.

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• 2000
  • 2000-03-31 JP JP2000098466A patent/JP4512872B2/ja not_active Expired - Lifetime
• 2001
  • 2001-03-29 US US09/821,622 patent/US6573018B2/en not_active Expired - Fee Related
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